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Dimethylamino-trifluor-phenyl-phosphoran, also known as O,O-dimethyl-O-(3-trifluoromethylphenyl)phosphorothioate, is an organophosphorus compound with the chemical formula C9H10F3NO3PS. It is a colorless to pale yellow liquid with a pungent odor and is used as an insecticide and acaricide in agriculture. The compound is effective against a wide range of pests, including aphids, mites, and whiteflies, due to its ability to inhibit acetylcholinesterase, an enzyme essential for the proper functioning of the nervous system in insects. As a result, it disrupts the nervous system of the target pests, leading to their paralysis and eventual death. However, it is important to note that the use of this chemical should be carried out with caution, as it can also pose risks to non-target organisms and the environment.

1077-47-0

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1077-47-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1077-47-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1077-47:
(6*1)+(5*0)+(4*7)+(3*7)+(2*4)+(1*7)=70
70 % 10 = 0
So 1077-47-0 is a valid CAS Registry Number.

1077-47-0Downstream Products

1077-47-0Relevant academic research and scientific papers

Phosphorus-fluorine chemistry. XIII. The adduct of nitrosyl fluoride with phenyltetrafluorophosphorane. New fluorophosphates

Schmutzler,Reddy

, p. 191 - 197 (2007/10/04)

Nitrosyl fluoride was found to react with phenyltetrafluorophosphorane to form a solid, thermally unstable 1:1 adduct. Evidence for the formulation of this adduct as a nitrosyl salt, NO+C6H5PF5-, based on various chemical reactions, is presented. The novel fluoroanions, R(Ar)PF5-, together with alkyl(aryl)dialkylaminotrifluorophosphoranes, R(Ar)PF3NR2, are also obtained in the form of stable dialkylammonium salts upon dialkylaminolysis of tetrafluorophosphoranes, R(Ar)PF4. The stereochemistry of the R(Ar)PF5- anions, and of the alkyl(aryl)dialkylaminotrifluorophosphoranes, based on n.m.r. spectroscopic studies, is discussed. In contrast to nitrosyl fluoride, nitryl fluoride reacted with phenyltetrafluorophosphorane with direct nitration of the aromatic ring.

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